gudid
Primary ID: Amplitude T4
Amplitude By Auditdata (UDI Amplitude T4)
Manufactured by Auditdata A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Amplitude By Auditdata - Primary ID Amplitude T4
Device Regulatory Overview
The Amplitude By Auditdata (Model/Catalog Number: Amplitude T4) is a medical device manufactured by Auditdata A/S. This product is indexed under FDA Product Code / Category Classification EWO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Amplitude T4
- Product Code / EMDN
- EWO
- Device Name
- Database Sync Date
- 2026-08-09 09:12:44
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Amplitude By Auditdata?
The registered manufacturer of record for Amplitude By Auditdata is Auditdata A/S.
What is the Primary UDI-DI identifier for Amplitude By Auditdata?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Amplitude T4.
What classification code is assigned to this device?
This device is registered under product classification code EWO.
Similar Classification Devices (EWO)
Other Devices by Auditdata A/S
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